4,5-dihydro-1H-pyrazole derivatives having potent CB1-antagonistic activity

ABSTRACT

The present invention relates to a group of novel 4,5-dihydro-1H-pyrazole derivatives which are potent cannabinoid (CB 1 ) receptor antagonists with utility for the treatment of diseases connected with disorders of the cannabinoid system. The compounds have the general formula (Ia) or (Ib) 
                         
wherein the symbols have the meanings given in the specification.
 
     The invention also relates to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component.

This application is a continuation of application Ser. No. 10/472,529, filed Sep. 24, 2003, which issued on Dec. 13, 2005, as U.S. Pat. No. 6,974,810, which is the National Stage of International Application No. PCT/EP02/10435, filed Sep. 17, 2002, the disclosures of each of which is incorporated herein by reference in their entirety. This application also claims benefit of priority under 35 U.S.C. § 119 of Application No. 01203849.3, filed in Europe on Sep. 21, 2001, the disclosure of which is also incorporated herein by reference in its entirety.

The present invention relates to a group of novel 4,5-dihydro-1H-pyrazole derivatives, to methods for the preparation of these compounds, and to pharmaceutical compositions containing one or more of these compounds as an active component.

The above mentioned 4,5-dihydro-1H-pyrazoles are potent cannabinoid (CB₁) receptor antagonists with utility for the treatment of disorders involving cannabinoid neurotransmission.

Cannabinoids are present in the Indian hemp Cannabis sativa and have been used as medicinal agents for centuries (Mechoulam, R. and Feigenbaum, J. J. Prog. Med. Chem. 1987, 24, 159). However, only within the past ten years the research in the cannabinoid area has revealed pivotal information on cannabinoid receptors and their (endogenous) agonists and antagonists. The discovery and the subsequent cloning of two different subtypes of cannabinoid receptors (CB₁ and CB₂) stimulated the search for novel cannabinoid receptor antagonists (Munro, S. et al., Nature 1993, 365, 61. Matsuda, L. A. and Bonner, T. I. Cannabinoid Receptors, Pertwee, R. G. Ed. 1995, 117, Academic Press, London). In addition, pharmaceutical companies became interested in the development of cannabinoid drugs for the treatment of diseases connected with disorders of the cannabinoid system (Consroe, P. Neurobiology of Disease 1998, 5, 534. Pop, E. Curr. Opin. In CPNS Investigational Drugs 1999, 1, 587. Greenberg, D. A. Drug News Perspect 1999, 12, 458. Pertwee, R. G., Progress in Neurobiology 2001, 63, 569). Hitherto, several CB₁ receptor antagonists are known. Sanofi disclosed their diarylpyrazole congeners as selective CB₁ receptor antagonists. A representative example is SR-141716A (Dutta, A. K. et al., Med. Chem. Res. 1994, 5, 54. Lan, R. et al., J. Med. Chem. 1999, 42, 769. Nakamura-Palacios, E. M. et al., CNS Drug Rev. 1999, 5, 43). CP-272871 is a pyrazole derivative, like SR141716A, but less potent and less CB₁ receptor subtype-selective than SR141716A (Meschler, J. P. et al., Biochem. Pharmacol. 2000, 60, 1315). Aminoalkylindoles have been disclosed as CB₁ receptor antagonists. A representative example is Iodopravadoline (AM-630), which was introduced in 1995. AM-630 is a moderately active CB₁ receptor antagonist, but sometimes behaves as a weak partial agonist (Hosohata, K. et al., Life Sc. 1997, 61, PL115). Researchers from Eli Lilly described aryl-aroyl substituted benzofurans as selective CB₁ receptor antagonists (e.g. LY-320135) (Felder, C. C. et al., J. Pharmacol. Exp. Ther. 1998, 284, 291). 3-Alkyl-5,5′-diphenylimidazolidinediones were described as cannabinoid receptor ligands, which were indicated to be cannabinoid antagonists (Kanyonyo, M. et al., Biorg. Med. Chem. Lett. 1999, 9, 2233). Aventis Pharma claimed diarylmethyleneazetidine analogs as CB₁ receptor antagonists (Mignani, S. et al., Patent FR 2783246, 2000; Chem. Abstr. 2000, 132, 236982). Tricyclic pyrazoles were claimed by Sanofi-Synthelabo as CB₁ antagonists (Barth, F. et al., Patent WO 0132663, 2001; Chem. Abstr. 2001, 134, 340504). Interestingly, many CB₁ receptor antagonists have been reported to behave as inverse agonists in vitro (Landsman, R. S. et al., Eur. J. Pharmacol. 1997, 334, R1). Reviews provide a nice overview of the cannabinoid research area (Mechoulam, R. et al., Prog. Med. Chem. 1998, 35, 199. Lambert, D. M. Curr. Med. Chem. 1999, 6, 635. Mechoulam, R. et al., Eur. J. Pharmacol. 1998, 359, 1. Williamson, E. M. and Evans, F. J. Drugs 2000, 60, 1303. Pertwee, R. G. Addiction Biology 2000, 5, 37. Robson, P. Br. J. Psychiatry 2001, 178, 107. Pertwee, R. G. Prog. Neurobiol. 2001, 63, 569. Goya, P and Jagerovic, N. Exp. Opin. Ther. Patents 2000, 10, 1529. Pertwee, R. G. Gut 2001, 48, 859).

It has now surprisingly been found that potent and selective antagonism of cannabinoid-CB₁ receptors is present in the novel 4,5-dihydro-1H-pyrazole derivatives of the formula (Ia) or (Ib), prodrugs thereof, tautomers thereof and salts thereof

wherein

-   -   R and R₁ independently represent phenyl, thienyl or pyridyl         which groups may be substituted with 1, 2 or 3 substituents Y,         which can be the same or different, from the group C₁₋₃-alkyl or         alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethylthio,         trifluoromethoxy, nitro, amino, mono- or dialkyl (C₁₋₂)-amino,         mono- or dialkyl (C₁₋₂)-amido, (C₁₋₃)-alkyl sulfonyl,         dimethylsulfamido, C₁₋₃-alkoxycarbonyl, carboxyl,         trifluoromethylsulfonyl, cyano, carbamoyl, sulfamoyl and acetyl,         or R and/or R₁ represent naphtyl,     -   R₂ represents hydrogen, hydroxy, C₁₋₃-alkoxy, acetyloxy or         propionyloxy,     -   R₃ represents a hydrogen atom or a branched or unbranched C₁₋₈         alkyl group or a C₃₋₇ cycloalkyl group which alkyl group or         cycloalkyl group may be substituted with a hydroxy group,     -   R₄ represents a hydrogen atom or a branched or unbranched         C₁₋₈alkyl, C₃₋₈ cycloalkyl, C₂₋₁₀ heteroalkyl, C₃₋₈ nonaromatic         heterocycloalkyl or C₄₋₁₀ nonaromatic heterocycloalkyl-alkyl         moiety which moieties may contain one or more heteroatoms from         the group (O, N, S), which moieties may be substituted with a         keto group, trifluoromethyl group, C₁₋₃ alkyl group, hydroxy,         amino, monoalkylamino, or dialkylamino group or a fluoro atom,         or R₄ represents an amino, hydroxy, phenoxy or benzyloxy group         or R₄ represents a branched or unbranched C₁₋₈ alkoxy, C₃₋₈         alkenyl, C₅₋₈ cycloalkenyl or C₆₋₉ cycloalkenylalkyl group which         groups may contain a sulphur, nitrogen or oxygen atom, a keto         group or —SO₂— group which C₁₋₈ alkoxy, C₃₋₈ alkenyl, C₅₋₈         cycloalkenyl or C₆₋₉ cycloalkenylalkyl groups may be substituted         with a hydroxy group, a trifluoromethyl group, an amino group, a         monoalkylamino group or dialkylamino group or a fluoro atom, or         R₄ represents a phenyl, benzyl, pyridyl, thienyl, pyridylmethyl         or phenethyl group wherein the aromatic rings may be substituted         with 1, 2 or 3 of the substituents Y, wherein Y has the meaning         as indicated above, or     -   R₄ represents a group NR₈R₉ with the proviso that R₃ represents         a hydrogen atom or a methyl group and wherein R₈ and R₉ are the         same or different and represent C₁₋₄ alkyl or C₂₋₄         trifluoroalkyl or R₈ and R₉—together with the nitrogen atom to         which they are bonded—form a saturated or un-saturated         heterocyclic moiety having 4 to 8 ring atoms which heterocyclic         moiety may contain an oxygen or sulphur atom or a keto group or         —SO₂— group or an additional nitrogen atom, which saturated or         unsaturated heterocyclic moiety may be substituted with a C₁₋₄         alkyl group or     -   R₃ and R₄—together with the nitrogen atom to which they are         bonded—form a saturated or unsaturated, monocyclic or bicyclic         heterocyclic moiety having 4 to 10 ring atoms, which         heterocyclic moiety may contain one or more atoms from the group         (O, N, S) or a keto group or —SO₂— group, which moiety may be         substituted with a C₁₋₄ alkyl, hydroxyalkyl, phenyl, thienyl,         pyridyl, amino, monoalkylaminoalkyl, dialkylaminoalkyl,         monoalkylamino, dialkylamino, aminoalkyl, azetidinyl,         pyrrolidinyl, piperidinyl or hexahydro-1H-azepinyl group,     -   R₅ and R₆ independently of each other represent a hydrogen atom         or a branched or unbranched C₁₋₈ alkyl or alkenyl group which         groups may contain one or more heteroatoms from the group (O, N,         S), a keto group or a —SO₂— group and which groups may be         substituted with a hydroxy or amino group, or R₅ and R₆         independently of each other represent a C₃₋₈ cycloalkyl group or         C₃₋₈ cycloalkenyl group which may contain one or more ring         heteroatoms from the group (O, N, S) or the —SO₂— group and         which groups may be substituted with a hydroxy group, alkyl         (C₁₋₃), the —SO₂— group, the keto group, amino group,         monoalkylamino group (C₁₋₃) or dialkylamino group (C₁₋₃), or     -   R₅ represents a naphtyl group or a phenyl group which phenyl         group may be substituted with 1, 2 or 3 substituents Y wherein Y         has the meaning as described hereinabove, with the proviso that         R₆ represents a hydrogen atom, or a branched or unbranched alkyl         group (C₁₋₅) which alkyl group may contain one or more         heteroatoms from the group (O, N, S) or the —SO₂— group and         which alkyl group may be substituted with a hydroxy, keto or         amino group, or     -   R₅ and R₆—together with the nitrogen atom to which they are         bonded—form a monocyclic, bicyclic or tricyclic alkyl or alkenyl         group which may contain ring heteroatoms from the group (O, N,         S), the keto or the SO₂ group and which monocyclic, bicyclic or         tricyclic alkyl or alkenyl group may be substituted with a         hydroxy group, alkyl (C₁₋₃) group, SO₂ group, keto group, amino         group, monoalkylamino group (C₁₋₃), dialkylamino group (C₁₋₃),         pyrrolidinyl group or piperidinyl group, which monocyclic,         bicyclic or tricyclic alkyl or alkenyl group may contain an         annelated phenyl group which annelated phenyl group may be         substituted with 1 or 2 substituents Y, wherein Y has the         meaning as described herein above,     -   R₇ represents branched or unbranched C₁₋₃alkyl.

At least one centre of chirality is present (at the C₄ position of the 4,5-dihydro-1H-pyrazole moiety) in the compounds of the formula (Ia) and (Ib). The invention relates both to racemates, mixtures of diastereomers and the individual stereoisomers of the compounds having formula (Ia) or (Ib). Particular compounds of interest of formula (Ia) or (Ib) have the absolute stereoconfiguration at the C₄ position of the 4,5-dihydro-1H-pyrazole moiety as represented by the formulas (1a*) and (1b*):

The invention also relates both to the E isomer, Z isomer and E/Z mixtures of compounds having formula (Ia) or (Ib).

The compounds of the invention can be brought into forms suitable for administration by means of usual processes using auxiliary substances and/or liquid or solid carrier materials.

Due to the potent CB₁ antagonistic activity the compounds according to the invention are suitable for use in the treatment of psychiatric disorders such as psychosis, anxiety, depression, attention deficits, memory disorders, cognitive disorders, appetite disorders, obesity, addiction, appetence, drug dependence and neurological disorders such as neurodegenerative disorders, dementia, dystonia, muscle spasticity, tremor, epilepsy, multiple sclerosis, traumatic brain injury, stroke, Parkinson's disease, Alzheimer's disease, epilepsy, Huntington's disease, Tourette's syndrome, cerebral ischaemia, cerebral apoplexy, craniocerebral trauma, stroke, spinal cord injury, neuroinflammatory disorders, plaque sclerosis, viral encephalitis, demyelinisation related disorders, as well as for the treatment of pain disorders, including neuropathic pain disorders, and other diseases involving cannabinoid neurotransmission, including the treatment of septic shock, glaucoma, cancer, diabetes, emesis, nausea, asthma, respiratory diseases, gastrointestinal disorders, gastric ulcers, diarrhoea and cardiovascular disorders.

The affinity of the compounds of the invention for cannabinoid CB₁ receptors was determined using membrane preparations of Chinese hamster ovary (CHO) cells in which the human cannabinoid CB₁ receptor is stably transfected in conjunction with [³H]CP-55,940 as radioligand. After incubation of a freshly prepared cell membrane preparation with the [³H]-ligand, with or without addition of compounds of the invention, separation of bound and free ligand was performed by filtration over glassfiber filters. Radioactivity on the filter was measured by liquid scintillation counting.

The cannabinoid CB₁ antagonistic activity of compounds of the invention was determined by functional studies using CHO cells in which human cannabinoid CB₁ receptors are stably expressed. Adenylyl cyclase was stimulated using forskolin and measured by quantifying the amount of accumulated cyclic AMP. Concomitant activation of CB₁ receptors by CB₁ receptor agonists (e.g. CP-55,940 or (R)-WIN-55,212-2) can attenuate the forskolin-induced accumulation of cAMP in a concentration-dependent manner. This CB₁ receptor-mediated response can be antagonised by CB₁ receptor antagonists such as the compounds of the invention.

Intermediates having formula (II) (see below) can be obtained according to methods known, for example: a) Francotte, E.; Tong, Z. Chem. Abstr. 126, 213598; b) Rempfler, H. and Kunz, W. Chem. Abstr. 113, 40432; c) Rempfler, H. and Kunz, W. Chem. Abstr. 107, 217473.

Intermediates having formula (III) wherein R₂ represents hydrogen (see below) can be obtained according to methods known, for example: a) EP 0021506; b) DE 2529689, c) Grosscurt, A. C. et al., J. Agric. Food Chem. 1979, 27, (2), 406.

Intermediates having formula (III) wherein R₂ represents a hydroxy group can be obtained by reacting a compound having formula (II) with hydrazine or hydrazine hydrate

This reaction, preferably carried out in an organic solvent such as ethanol, yields a compound having formula (III) wherein R₂ represents a hydroxy group.

Suitable synthetic routes for the compounds of the invention are the following:

Synthetic Route A

Step 1: reaction of a compound having formula (III)

with a compound having formula (IV).

This reaction is preferably carried out in an organic solvent, such as for example dichloromethane, and yields a compound having formula (V) wherein R, R₁, R₂, R₅ and R₆ have the meaning as described above for compound (Ia), and which are new.

Step 2: reaction of a compound having formula (V) with a compound R₇—X, wherein X represents a leaving group, for example an iodide group, and R₇ has the meaning as described above for (Ib) gives a compound having formula (Ib).

This reaction is preferably carried out in the presence of a base, for example triethylamine.

Step 3: reaction of a compound having formula (Ib) with an amine having formula HNR₃R₄ wherein R₃ and R₄ have the meanings as described above, analogous to the method described in Synth. Commun. 1996, 26, (23), 4299.

This reaction gives a compound having formula (Ia).

Synthetic Route A1

Step 1: Reaction of a compound having formula (V)

with an amine having formula HNR₃R₄ wherein R₃ and R₄ have the meanings as described above in the presence of a mercury (II) salt, for example HgCl₂, gives a compound having formula (Ia).

This reaction is preferably carried out in an organic solvent, such as for example acetonitrile, analogous to the method described in Synth. Commun. 1996, 26, (23), 4299.

Synthetic Route A2

Step 1: reaction of a compound having formula (III)

with a isocyanate derivative having formula (VI), followed by treatment with an amine HNR₅R₆

This reaction is preferably carried out in an organic solvent like dichloromethane, and yields a compound having formula (VII). Compounds having formula (VII) wherein R, R₁, R₂, R₅ and R₆ have the meaning as described herein above for compound (Ia) are new.

Step 2: reaction of a compound having formula (VII) with a halogenating agent, such as for example PCl₅, gives a compound having formula (VIII)

wherein R₁₀ represents a halogen atom, for example a chloro atom. This reaction is preferably carried out in an organic solvent such as chlorobenzene.

Compounds having formula (VIII) wherein R, R₁, R₂, R₅ and R₆ have the meanings as described above for compound (Ia) and wherein R₁₀ represents a halogen atom, are new.

Step 3: reaction, preferably carried out in an inert organic solvent such as dichloromethane, of a compound having formula (VIII) with an amine having formula HNR₃R₄ wherein R₃ and R₄ have the meanings as described above gives a compound having formula (Ia).

Synthetic Route A3

Step 1: reaction of a compound having formula (III)

with a compound having formula (IX)

gives a compound having formula (Ib), (see e.g. Chem. Ber. 1966, 99, 2885 and Chem. Ztg. 1984, 108, (12), 404).

The preparation of the compounds is illustrated in the following examples.

EXAMPLE 1 3-(4-Chlorophenyl)-N′-(((ethyl)propylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine

Part A: To a stirred solution of ((ethyl)propylamino)sulfonyl isothiocyanate (5.98 gram, 25.4 mmol) in dry dichloromethane in a nitrogen atmosphere is added of 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole (6.52 gram, 25.4 mmol). After stirring for 90 minutes the resulting solution is concentrated in vacuo and purified by column chromatography (CH₂Cl₂, silicagel, R_(f) ˜0.45). The resulting solid is recrystallized from diethyl ether to give 3-(4-chlorophenyl)-N-(((ethyl)propylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyra-zole-1-thiocarboxamide (6.57 gram, 56% yield). Melting point: 144-146° C.

Part B: To a stirred suspension of 3-(4-chlorophenyl)-N-(((ethyl)propyl-amino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-thiocarboxamide (2.32 gram, 5 mmol) in acetonitrile (20 mL) is added cold methylamine (4 mL). To the resulting solution is added a solution of HgCl₂ (1.5 gram) in acetonitrile (10 mL). The resulting black suspension is stirred for four hours. The precipitate is removed by filtration. The filtrate is concentrated in vacuo, dissolved in dichloromethane and successively washed with aqueous 0.5 N NaOH solution and water, dried over Na₂SO₄, filtered and concentrated in vacuo. The resulting oil is crystallized from diethyl ether to give 3-(4-chlorophenyl)-N′-(((ethyl)propylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine (1.78 gram, 77% yield). Melting point (MP):129-131° C.

In an analogous manner the compounds having formula (Ia) listed below have been prepared:

2. 3-(4-Chlorophenyl)-N′-(((ethyl)methylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 112-115° C.

3. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-(2-hydroxyethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 104-106° C.

4. 3-(4-Chlorophenyl)-N-(2-hydroxyethyl)-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS (ESI+): 490 (MH⁺).

5. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-(2-(morpholin-4-yl)ethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS (ESI+): 547 (MH⁺))

6. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-(2-(morpholin-4-yl)ethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

7. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-(2-(dimethylamino)ethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS (ESI+): 505 (MH⁺)).

8. 3-(4-Chlorophenyl)-N-(3-(dimethylamino)propyl)-N′-((dimethylamino)sulfo-nyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

9. 3-(4-Chlorophenyl)-N-(2-(piperidin-1-yl)ethyl)-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS (ESI+): 557 (MH⁺)).

10. 3-(4-Chlorophenyl)-N-(2-(morfolin-4-yl)ethyl)-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS (ESI+): 559 (MH⁺)); MP: 174-176° C.

11. 3-(4-Chlorophenyl)-N-(2-(dimethylamino)ethyl)-N′-((dimethylamino)sulfo-nyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

12. 3-(4-Chlorophenyl)-N-(2-(diethylamino)ethyl)-N′-((dimethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

13. 3-(4-Chlorophenyl)-N-(3-(dimethylamino)propyl)-N′-((diethylamino)sulfo-nyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MS(ESI+):519 (MH⁺).

14. 3-(4-Chlorophenyl)-N-(2-(diethylamino)ethyl)-N′-((diethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine hemifumarate. MP: 182-185° C.

15. 3-(4-Chlorophenyl)-N-(2-(dimethylamino)ethyl)-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

16. 3-(4-Chlorophenyl)-N-(2-(diethylamino)ethyl)-N′-((pyrrolidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

17. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-(1-methylpiperidin-4-yl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

18. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-(2-hydroxyethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 123-126° C.

19. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous. R_(f) ˜0.4 (diethyl ether).

20. 3-(4-Chlorophenyl)-N′-(((ethyl)propylamino)sulfonyl)-N-Methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 129-131° C.

21. 3-(4-Chlorophenyl)-N-methyl-N′-((pyrrolidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous. R_(f) ˜0.3 (MTBE).

22. 3-(4-Chlorophenyl)-N-methyl-N′-(((methyl)propylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 132-134° C.

23. 3-(4-Chlorophenyl)-N,N-dimethyl-N′-((pyrrolidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous. R_(f) ˜0.25 (MTBE).

24. 3-(4-Chlorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 175-177° C.

25. 3-(4-Chlorophenyl)-N′-((hexahydro-1H-azepin-1-yl)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

26. 3-(4-Chlorophenyl)-N′-((dipropylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 141-142° C.

27. 3-(4-Chlorophenyl)-N′-(((isopropyl)methylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 134-136° C.

28. 3-(4-Chlorophenyl)-N-methyl-N′-((octahydroazocin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 165-168° C.

29. 3-(4-Chlorophenyl)-N-ethyl-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

30. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 166-168° C.

EXAMPLE 31 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-propyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine

Part A: To a stirred solution of chlorosulfonyl isocyanate (1.73 mL, 20 mmol) in dry dichloromethane (20 mL) is very slowly added a solution of 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole (5.13 gram, 20 mmol) in dry dichloromethane (125 mL) at −5° C. After stirring for 30 minutes the reaction mixture is allowed to attain room temperature and stirred for another 2 hours. After cooling to 0° C. liquid dimethylamine (5 mL) is added and the resulting solution is stirred for another hour at 0° C. and for 2 hours at room temperature. The solution is washed with water, filtered over hyflo and concentrated in vacuo. Flash chromatography (MTBE, R_(f) ˜0.3) gives 3-(4-chlorophenyl)-N-((dimethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamide (4.75 g, 58%). MP: 210-212° C.

Part B: A mixture of 3-(4-chlorophenyl)-N-((dimethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamide (1.47 gram, 3.62 mmol) and phosphorus pentachloride (0.80 gram, 3.84 mmol) in chlorobenzene (20 mL) is heated at reflux temperature for 1 hour. After thorough concentration in vacuo, the formed 3-(4-chlorophenyl)-N-((dimethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidoyl chloride is suspended in dry dichloromethane and reacted with cold n-propylamine (1.0 mL) at 0° C. After stirring for 1 hour, the mixture is dissolved in ethyl acetate and washed with water and concentrated in vacuo. The residue is purified by column chromatography (dichloromethane/acetone=19/1 (v/v), R_(f) ˜0.35) to give an oil (0.82 g). Crystallisation from diethyl ether, followed by recrystallisation from ethanol gives 3-(4-chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-propyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine (0.38 gram, 23% yield). MP: 127-129° C.

In an analogous manner the compounds having formula (Ia) listed below have been prepared:

32. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-(2-fluoroethyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 128-131° C.

33. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-4-phenyl-N-(2,2,2-trifluoroethyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 158-159° C.

34. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methoxy-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 170-172° C.

EXAMPLE 35 3-(4-Chlorophenyl)-N-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester

Part A: To a stirred solution of (piperidin-1-yl)sulfonyl isothiocyanate (54.77 g, 266 mmol) in dry dichloromethane (900 mL) in a nitrogen atmosphere is added 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole (68.3 gram, 266 mmol). After stirring for 16 hours an additional amount of dichloromethane is added. The resulting solution is twice washed with water, dried over Na₂SO₄, and concentrated in vacuo. After addition of MTBE, the residue crystallizes. The crystalline material is collected and washed with MTBE to give 3-(4-chlorophenyl)-4-phenyl-N-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-thiocarboxamide (77.6 gram, 63% yield).

Part B: To a stirred solution of 3-(4-chlorophenyl)-4-phenyl-N-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-thiocarboxamide (30 gram, 64.9 mmol) in acetone (1 L) is added triethylamine (18.0 mL, 130 mmol). To the resulting yellow solution is added methyl iodide (9.12 g, 64 mmol) and the resulting solution is stirred for 16 hours at room temperature. The formed precipitate is removed by filtration. The filtrate is washed with water, concentrated in vacuo to give a yellow solid. Recrystallisation from MTBE gives 3-(4-chlorophenyl)-N-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester (27.9 gram, 90% yield). MP: 192-194° C.

In an analogous manner the compounds having formula (Ib) listed below have been prepared:

36. 3-(4-Chlorophenyl)-N-((dimethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 159-160° C.

37. 3-(4-Chlorophenyl)-N-((diethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 141-143° C.

38. 3-(4-Chlorophenyl)-4-phenyl-N-((1,2,3,4-tetrahydroisoquinolin-2-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 143-145° C.

39. 3-(4-Chlorophenyl)-N-(((ethyl)phenylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 143-146° C.

40. 3-(4-Chlorophenyl)-N-((diethylamino)sulfonyl)-4-hydroxy-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

41. 3-(4-Chlorophenyl)-N-((diethylamino)sulfonyl)-4-(pyridin-4-yl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

42. 3-(4-Chlorophenyl)-N-((piperidin-1-yl)sulfonyl)-4-(3-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

43. 3-(4-Chlorophenyl)-N-((dimethylamino)sulfonyl)-4-(3-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

44. 3-(4-Chlorophenyl)-N-(((ethyl)methylamino)sulfonyl)-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP:133-136° C.

45. 3-(4-Chlorophenyl)-N-((piperidin-1-yl)sulfonyl)-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 182-185° C.

46. 3-(4-Chlorophenyl)-N-((morpholin-4-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 202-204° C.

47. 3-(4-Chlorophenyl)-4-(2-fluorophenyl)-N-((morpholin-4-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP:205-207° C.

48. 3-(4-Chlorophenyl)-4-(2-fluorophenyl)-N-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 196-198° C.

49. 3-(4-Chlorophenyl)-4-(2-fluorophenyl)-N-(dimethylamino)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 181-183° C.

50. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N-((morpholin-4-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP:231-233° C.

51. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP:221-225° C.

52. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N-((dimethylamino)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP:181-185° C.

53. 3-(4-Chlorophenyl)-N-((1,1-dioxidothiomorpholin-4-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 216-217° C.

54. 3-(5-Chlorothien-2-yl)-N-((diethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

EXAMPLE 55 3-(4-Chlorophenyl)-N-methyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine

To a cooled mixture (<0° C.) of 3-(4-chlorophenyl)-N-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester (10.0 gram, 21 mmol) in methanol (75 mL) is added cold methylamine (15 mL). The resulting mixture is allowed to attain room temperature and stirred for 3 hours at 50° C. After cooling to room temperature the mixture is concentrated in vacuo, dissolved in dichloromethane, washed twice with water, dried over Na₂SO₄, filtered and concentrated in vacuo. Subsequent flash chromatography (EtOAc/MeOH/NH₄OH (25% aq.)=95/5/0.5 (v/v)), followed by recrystallisation from diisopropyl ether gives 3-(4-chlorophenyl)-N-methyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine (7.87 gram, 81% yield) as a white solid. MP: 175-177° C.

In an analogous manner the compounds having formula (Ia) listed below—including those in table 1—have been prepared:

56. 3-(4-Chlorophenyl)-N-cyclopropyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 142-144° C.

57. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-methyl-4-hydroxy-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 180-182° C.

58. 3-(5-Chlorothien-2-yl)-N′-((diethylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 122-123° C.

59. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-isopropyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 169-170° C.

60. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-(1-methylpiperidin-4-yl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 144-146° C.

61. 3-(4-Chlorophenyl)-N-cyclopropyl-N′-((diethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 150-151° C.

62. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-ethyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 116-119° C.

63. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N,N-dimethyl-4-hydroxy-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 135-137° C.

64. N′-((Diethylamino)sulfonyl)-N,N-dimethyl-3-(4-fluorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 159-160° C.

65. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-isopropyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 81-85° C.

66. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-ethyl, N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

67. 3-(4-Chlorophenyl)-N-ethyl, N-methyl-N′-((piperidin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 178° C.

68. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-ethyl-4-hydroxy-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 162-165° C.

69. 3-(4-Chlorophenyl)-N-methyl-N′-((1,2,3,4-tetrahydroisoquinolin-2-yl)sulfo-nyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. Amorphous.

70. 3-(4-Chlorophenyl)-N′-(((ethyl)phenylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 145-147° C.

71. N′-((Diethylamino)sulfonyl)-3-(4-chlorophenyl)-N-methyl-4-(pyridin-4-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 109-111° C.

72. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 157-159° C.

73. 3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-methyl-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 85-89° C.

74. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4-(pyridin-4-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 178-182° C.

75. 3-(4-Chlorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4-(3-(trifluoro-methyl)phenyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 168-170° C.

76. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4-(3-(trifluoro-methyl)phenyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 65-68° C.

77. 3-(4-Chlorophenyl)-N′-(((ethyl)methylamino)sulfonyl)-N-methyl-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 125-128° C.

78. 3-(4-Chlorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4-(pyridin-3-yl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 174-177° C.

79. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N-methyl-N′-((morpholin-4-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 223-235° C.

80. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 214-216° C.

81. 3-(4-Chlorophenyl)-4-(2,6-difluorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 260-263° C.

82. 3-(4-Chlorophenyl)-4-(3-fluorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 170° C.

83. 3-(4-Chlorophenyl)-4-(2-fluorophenyl)-N-methyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 223-225° C.

84. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-4-(2-fluorophenyl)-N-methyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 173-175° C.

85. 3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-4-(3-fluorophenyl)-N-methyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 110° C.

86. 3-(4-Chlorophenyl)-4-(2-fluorophenyl)-N-methyl-N′-((morpholin-4-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 165-168° C.

87. 3-(4-Chlorophenyl)-N′-((1,1-dioxidothiomorpholin-4-yl)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 268-271° C.

88. 3-(4-Chlorophenyl)-N′-((4-hydroxypiperidin-1-yl)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. MP: 80° C.

TABLE 1

Example: R₁₁ R₁₂ MP (° C.) Salt form 89: 4-Methyl- Dimethylamino 197-200 0.5 Fumarate 1,4-diaze- pan-1-yl 90: 1,4-Diaze- Piperidin-1-yl Amorphous pan-1-yl 91: 1,4-Diaze- Dimethylamino Amorphous pan-1-yl 92: 4-Methyl- Piperidin-1-yl 159-164 1,4-diaze- pan-1-yl 93: 4-Methyl- Dimethylamino 191-193 piperazin- 1-yl

EXAMPLE 94 3-(4-Chlorophenyl)-N-((4-methylpiperazin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester

Part A: A stirred mixture of 3-(4-chlorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole (3.21 gram, 11.3 mmol), [(4-methylpiperazin-1-yl)sulfonyl]dithioimido-carbonic acid dimethyl ester (3.08 gram, 12.0 mmol) and pyridine (25 mL) is heated at 100° C. for 24 hours in a nitrogen atmosphere. After cooling to room temperature the mixture is concentrated in vacuo, water is added and the resulting mixture is extracted with dichloromethane. The dichloromethane extract is washed twice with water, dried over Na₂SO₄, filtered and concentrated in vacuo. Subsequent flash chromatographic purification gives 3-(4-chlorophenyl)-N-((4-methylpiperazin-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester (4.24 gram, 76% yield) as an amorphous solid. (R_(f) ˜0.1, EtOAc/methanol=95/5 (v/v)).

In an analogous manner the compounds having formula (Ib) listed below have been prepared:

95. 3-(4-Chlorophenyl)-N-(((2-(dimethylamino)ethyl)ethylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester.

MP: 158° C.

96. N-((Diethylamino)sulfonyl)-3-(4-fluorophenyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

R_(f) ˜0.4 (MTBE).

97. 3-(4-Chlorophenyl)-N-(([1,4′]bipiperidin-1′-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. MP: 245° C.

98. 3-(4-Chlorophenyl)-N-(((1-methylpiperidin-4-yl)methylamino)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Oil. R_(f) ˜0.15 (methanol/dichloromethane=5/95 (v/v)).

99. 3-(4-Chlorophenyl)-N-((4-methyl-1,4-diazepan-1-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboximidothioic acid methyl ester. Amorphous.

R_(f) ˜0.10 (methanol/dichloromethane=5/95 (v/v)).

EXAMPLE 100 (−)-(4S)-3-(4-Chlorophenyl)-N-methyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine

(−)-(4S)-3-(4-Chlorophenyl)-N-methyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine (3.8 gram, 8.3 mol)) ([α²⁵ _(D)]=−139°, c=0.006, MeOH) was obtained as an amorphous solid via chiral chromatographic separation of racemic 3-(4-chlorophenyl)-N-methyl-4-phenyl-N′-((piperidin-1-yl)sulfonyl)-4,5-dihydro-1H-pyrazole-1-carboxamidine (7.87 gram, 17.1 mmol) using a chiral stationary phase Chiralpak AD. The mobile phase consisted of methanol/diethylamine=999/1 (v/v).

In an analogous manner the optically pure compounds listed below have been prepared from the corresponding racemates:

101. (−)-(4S)-3-(4-Chlorophenyl)-N′-((diethylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine (Chiral stationary phase: Chiralcel OD). Mobile phase consisted of hexane/2-propanol=80/20 (v/v). ([α²⁵ _(D)]=−147°, c=0.01, MeOH). Amorphous.

102. (−)-(4S)-3-(4-Chlorophenyl)-N′-((dimethylamino)sulfonyl)-N-methyl-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine (Chiral stationary phase: Chiralpak AD). The mobile phase consisted of methanol/diethylamine=999/1 (v/v). ([α²⁵ _(D)]=−171°, c=0.005, MeOH). Amorphous.

103. (−)-(4S)-3-(4-Chlorophenyl)-N-methyl-N′-((morpholin-4-yl)sulfonyl)-4-phenyl-4,5-dihydro-1H-pyrazole-1-carboxamidine. ([α²⁵ _(D)]=−144°, c=0.01, MeOH). (Chiral stationary phase: Chiralpak AD). The mobile phase consisted of ethanol. Amorphous. 

1. A compound of formula (I):


2. A pharmaceutical composition comprising a pharmaceutically effective amount of a compound of formula (I), as claimed in claim 1, and at least one auxiliary substance, liquid carrier material, or solid carrier material, or a mixture of two or more of the foregoing. 